Yokoyama Y - Search Results

1

De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies.

Wakita Y, Narahara K, Tsuji K, Yokoyama Y, Ninomiya S, Murakami R, Kikkawa K, Seino Y. Wakita Y, et al. Among authors: yokoyama y. Hum Genet. 1992 Mar;88(5):596-8. doi: 10.1007/BF00219353. Hum Genet. 1992. PMID: 1551663

2

Terminal 22q deletion associated with a partial deficiency of arylsulphatase A.

Narahara K, Takahashi Y, Murakami M, Tsuji K, Yokoyama Y, Murakami R, Ninomiya S, Seino Y. Narahara K, et al. Among authors: yokoyama y. J Med Genet. 1992 Jun;29(6):432-3. doi: 10.1136/jmg.29.6.432. J Med Genet. 1992. PMID: 1352356 Free PMC article. Review.

3

Tissue-specific mosaicism for trisomy 21 and congenital heart disease.

Yokoyama Y, Narahara K, Kamada M, Tsuji K, Seino Y. Yokoyama Y, et al. J Pediatr. 1992 Jul;121(1):80-2. doi: 10.1016/s0022-3476(05)82547-8. J Pediatr. 1992. PMID: 1385628

4

Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation.

Yokoyama Y, Narahara K, Tsuji K, Ninomiya S, Seino Y. Yokoyama Y, et al. Hum Genet. 1992 Sep-Oct;90(1-2):177-8. doi: 10.1007/BF00210770. Hum Genet. 1992. PMID: 1427774

5

Case of ovarian dysgenesis and dilated cardiomyopathy supports existence of Malouf syndrome.

Narahara K, Kamada M, Takahashi Y, Tsuji K, Yokoyama Y, Ninomiya S, Seino Y. Narahara K, et al. Among authors: yokoyama y. Am J Med Genet. 1992 Oct 1;44(3):369-73. doi: 10.1002/ajmg.1320440320. Am J Med Genet. 1992. PMID: 1488988 Review.

6

Growth hormone deficiency and empty sella syndrome in a boy with dup(X) (q13.3----q21.2).

Yokoyama Y, Narahara K, Tsuji K, Moriwake T, Kanzaki S, Murakami M, Namba H, Ninomiya S, Higuchi J, Seino Y. Yokoyama Y, et al. Am J Med Genet. 1992 Mar 1;42(5):660-4. doi: 10.1002/ajmg.1320420506. Am J Med Genet. 1992. PMID: 1632433

7

Unique karyotypes in two patients with Prader-Willi syndrome.

Narahara K, Hiramoto K, Murakami M, Miyake S, Tsuji K, Yokoyama Y, Namba H, Ninomiya S, Murakami R, Seino Y. Narahara K, et al. Among authors: yokoyama y. Am J Med Genet. 1992 Mar 1;42(5):671-7. doi: 10.1002/ajmg.1320420509. Am J Med Genet. 1992. PMID: 1632436

8

Gardner syndrome in a boy with interstitial deletion of the long arm of chromosome 5.

Kobayashi T, Narahara K, Yokoyama Y, Ueyama S, Mohri O, Fujii T, Fujimoto M, Ohtsuki S, Tsuji K, Seino Y. Kobayashi T, et al. Among authors: yokoyama y. Am J Med Genet. 1991 Dec 15;41(4):460-3. doi: 10.1002/ajmg.1320410416. Am J Med Genet. 1991. PMID: 1776638 Review.

9

Assignment of human porphobilinogen deaminase to 11q24.1----q24.2 by in situ hybridization and gene dosage studies.

Namba H, Narahara K, Tsuji K, Yokoyama Y, Seino Y. Namba H, et al. Among authors: yokoyama y. Cytogenet Cell Genet. 1991;57(2-3):105-8. doi: 10.1159/000133123. Cytogenet Cell Genet. 1991. PMID: 1914516

10

Specification of small distal 6q deletions in two patients by gene dosage and in situ hybridization study of plasminogen and alpha-L-fucosidase 2.

Narahara K, Tsuji K, Yokoyama Y, Namba H, Murakami M, Matsubara T, Kasai R, Fukushima Y, Seki T, Wakui K, et al. Narahara K, et al. Among authors: yokoyama y. Am J Med Genet. 1991 Sep 1;40(3):348-53. doi: 10.1002/ajmg.1320400322. Am J Med Genet. 1991. PMID: 1951444

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